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大鼠肝脏中1-邻苯二甲酰基5-氟尿嘧啶的代谢及苯巴比妥对酶的诱导作用。

Metabolism of 1-phthalidyl 5-fluorouracil in rat liver and enzyme induction by phenobarbital.

作者信息

Tonda K, Kamata S, Hirata M

出版信息

Xenobiotica. 1987 Jun;17(6):759-68. doi: 10.3109/00498258709043983.

Abstract
  1. When 1-phthalidyl 5-fluorouracil (PH-FU) was incubated with isolated rat hepatocytes, 5-fluorouracil, 2-carboxybenzaldehyde (CBA) and alpha-hydroxymethylbenzoic acid (HMB) were detected as the major metabolites. 2. The enzymes involved in the metabolism of PH-FU, PH-FU hydrolase and CBA reductase are cytosolic and were induced by treating the rats with phenobarbital (PB). Treatment of rats with 3-methylcholanthrene (3-MC) did not affect either enzyme activity. 3. The PB-induced PH-FU hydrolase was inhibited by NADH and several aldehydes, while NAD stimulated the hydrolase and protected it from inactivation by SH reagents. 4. Study in vivo revealed that treatment of rats with PB accelerated the metabolism of PH-FU in the liver and markedly decreased the blood PH-FU after its oral administration to rats, which resulted in reduction of the anti-tumour activity of PH-FU. This activity was not affected by treatment of the rats with 3-MC.
摘要
  1. 当1-酞嗪基5-氟尿嘧啶(PH-FU)与分离的大鼠肝细胞一起孵育时,检测到5-氟尿嘧啶、2-羧基苯甲醛(CBA)和α-羟甲基苯甲酸(HMB)为主要代谢产物。2. 参与PH-FU代谢的酶,即PH-FU水解酶和CBA还原酶存在于胞质中,并且通过用苯巴比妥(PB)处理大鼠而被诱导。用3-甲基胆蒽(3-MC)处理大鼠对这两种酶的活性均无影响。3. PB诱导的PH-FU水解酶被NADH和几种醛抑制,而NAD刺激该水解酶并保护其免受SH试剂的失活作用。4. 体内研究表明,用PB处理大鼠会加速肝脏中PH-FU的代谢,并在给大鼠口服PH-FU后显著降低血液中的PH-FU,这导致PH-FU的抗肿瘤活性降低。该活性不受用3-MC处理大鼠的影响。

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